FDA applicant

Pulse Metric, Inc.

San Diego, CA5 decisions1991–20020 recalls

FDA records 5 decisions for Pulse Metric, Inc. (San Diego, CA) from 1991 to 2002: 5 510(k) clearances. All are in product code DXN (System, Measurement, Blood-Pressure…). No recall is linked to its devices.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

FIG. A — Illustration, cardiovascular panel, where it files most

How often FDA has decided Pulse Metric, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Pulse Metric, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Pulse Metric, Inc. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Pulse Metric, Inc.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

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Other applicant names beginning “Pulse”

FDA records each applicant name separately; these may or may not be the same firm.

Pulse Biosciences, Inc. 7 Pulse Time Products, Ltd. 6 Pulse Biomedical, Inc. 3 Pulse Scientific, Inc. 3 Pulse Medical Instruments 1 Pulse Life, Inc. 1 Pulse Med, Inc. 1

Pulse Metric, Inc.

Which product codes does it file in?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?

Other applicant names beginning “Pulse”